Sato T, Ueda T, Kon H, Yagihashi S, Kotanagi H
Department of Surgery, Hokushu Chuo Hospital, Akita, Japan.
J Gastroenterol. 1995 Dec;30(6):779-82. doi: 10.1007/BF02349647.
We describe a case of mucinous cystadenoma of the appendix with perityphlic granuloma. The patient developed a hard palpable mass in the right lower quadrant and barium enema induced irregular bowel wall at the cecum. Based on a preoperative diagnosis of carcinoma of the appendix, we performed a laparotomy. On operation, we found a tumor mass in the region of the appendix; the mass adhered strongly to the retroperitoneum and cecum. Right hemicolectomy was carried out on a diagnosis of carcinoma of the appendix. Microscopic examination revealed mucinous cystadenoma of the appendix with perityphlic granuloma. Mucinous cystadenoma in the appendix is a rare tumor. In this patient, the tumor was accompanied by granuloma formation in adjacent tissues because of mucin expelled from the appendix. This case emphasizes that granuloma formation can make of difficult to differentiate mucinous cystadenoma in the appendix from cancer.
我们描述了一例伴有盲肠周围肉芽肿的阑尾黏液性囊腺瘤病例。患者右下腹出现一个可触及的硬块,钡灌肠显示盲肠肠壁不规则。基于阑尾癌的术前诊断,我们进行了剖腹手术。术中,我们在阑尾区域发现一个肿瘤肿块;该肿块与腹膜后和盲肠紧密粘连。基于阑尾癌的诊断实施了右半结肠切除术。显微镜检查显示为伴有盲肠周围肉芽肿的阑尾黏液性囊腺瘤。阑尾黏液性囊腺瘤是一种罕见的肿瘤。在该患者中,由于阑尾排出的黏液,肿瘤在相邻组织中伴有肉芽肿形成。该病例强调肉芽肿形成会使阑尾黏液性囊腺瘤与癌症的鉴别变得困难。